These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

243 related articles for article (PubMed ID: 24316408)

  • 21. Neutropenia, hypogammaglobulinemia, and pneumonia: A case of WHIM syndrome.
    Saettini F; Notarangelo LD; Biondi A; Bonanomi S
    Pediatr Int; 2018 Mar; 60(3):318-319. PubMed ID: 29575308
    [No Abstract]   [Full Text] [Related]  

  • 22. Immune deficiency disorders involving neutrophils.
    Spickett GP
    J Clin Pathol; 2008 Sep; 61(9):1001-5. PubMed ID: 18755725
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Late onset of primary immune deficiencies].
    Bussone G; Mouthon L
    Presse Med; 2010 Feb; 39(2):196-207. PubMed ID: 19481902
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Merkel cell carcinoma in a patient with GATA2 deficiency: a novel association with primary immunodeficiency.
    Crall C; Morley KW; Rabinowits G; Schmidt B; Dioun Broyles A; Huang JT
    Br J Dermatol; 2016 Jan; 174(1):169-71. PubMed ID: 26252413
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Spurious white blood cell count from a new automated Sysmex XN hematology analyzer.
    Tantanate C
    Int J Lab Hematol; 2014 Dec; 36(6):e86-7. PubMed ID: 24628773
    [No Abstract]   [Full Text] [Related]  

  • 26. STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutation.
    Halacli SO; Ayvaz DC; Sun-Tan C; Erman B; Uz E; Yilmaz DY; Ozgul K; Tezcan İ; Sanal O
    Clin Immunol; 2015 Dec; 161(2):316-23. PubMed ID: 26117625
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Well tolerated neutropenia and monocytopenia (author's transl)].
    Rewald E
    Sangre (Barc); 1977; 22(3):388-92. PubMed ID: 867216
    [No Abstract]   [Full Text] [Related]  

  • 28. GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia.
    Ishida H; Imai K; Honma K; Tamura S; Imamura T; Ito M; Nonoyama S
    Eur J Pediatr; 2012 Aug; 171(8):1273-6. PubMed ID: 22430350
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Primary immunodeficiencies.
    Worley K; White JA
    J La State Med Soc; 1992 Nov; 144(11):497-500. PubMed ID: 1431479
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Evaluation of primary immunodeficiency disease in children.
    Reust CE
    Am Fam Physician; 2013 Jun; 87(11):773-8. PubMed ID: 23939499
    [TBL] [Abstract][Full Text] [Related]  

  • 31. WHIM syndrome: congenital immune deficiency disease.
    Kawai T; Malech HL
    Curr Opin Hematol; 2009 Jan; 16(1):20-6. PubMed ID: 19057201
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A Sherlock Approach to a Kindred With a Variable Immunohematologic Phenotype.
    Walkovich K; Grunebaum E
    J Allergy Clin Immunol Pract; 2022 Jul; 10(7):1714-1722. PubMed ID: 35470097
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Recent advances in understanding the pathogenesis and management of reticular dysgenesis.
    Hoenig M; Pannicke U; Gaspar HB; Schwarz K
    Br J Haematol; 2018 Mar; 180(5):644-653. PubMed ID: 29270983
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Neutropenia in Iranian patients with primary immunodeficiency disorders.
    Rezaei N; Farhoudi A; Pourpak Z; Aghamohammadi A; Moin M; Movahedi M; Gharagozlou M
    Haematologica; 2005 Apr; 90(4):554-6. PubMed ID: 15820955
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Tetralogy of fallot is an uncommon manifestation of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome.
    Badolato R; Dotta L; Tassone L; Amendola G; Porta F; Locatelli F; Notarangelo LD; Bertrand Y; Bachelerie F; Donadieu J
    J Pediatr; 2012 Oct; 161(4):763-5. PubMed ID: 22748845
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Immunodeficiency Presenting as an Undiagnosed Disease.
    Routes JM; Verbsky JW
    Pediatr Clin North Am; 2017 Feb; 64(1):27-37. PubMed ID: 27894450
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Flow cytometry in the diagnosis of the primary immunodeficiencies].
    García Rodríguez MC; Cambronero Martínez R; Ferreira Cerdán A; Fontán Casariego G
    Sangre (Barc); 1999 Apr; 44(2):127-33. PubMed ID: 10382322
    [No Abstract]   [Full Text] [Related]  

  • 38. Diversity in Serine/Threonine Protein Kinase-4 Deficiency and Review of the Literature.
    Cagdas D; Halacli SO; Tan C; Esenboga S; Karaatmaca B; Cetinkaya PG; Balcı-Hayta B; Ayhan A; Uner A; Orhan D; Boztug K; Ozen S; Topaloglu R; Sanal O; Tezcan I
    J Allergy Clin Immunol Pract; 2021 Oct; 9(10):3752-3766.e4. PubMed ID: 34146746
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A novel G6PC3 gene mutation in severe congenital neutropenia: pancytopenia and variable bone marrow phenotype can also be part of this syndrome.
    Arikoglu T; Kuyucu N; Germeshausen M; Kuyucu S
    Eur J Haematol; 2015 Jan; 94(1):79-82. PubMed ID: 24750412
    [TBL] [Abstract][Full Text] [Related]  

  • 40. WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure.
    Heusinkveld LE; Majumdar S; Gao JL; McDermott DH; Murphy PM
    J Clin Immunol; 2019 Aug; 39(6):532-556. PubMed ID: 31313072
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.